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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286794Generated: November 1, 2026

Isopropyl iodide → HCID 54272250, compound

https://huagongshe.com/reaction/2286794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant3-Butenoic acid, 4-phenyl-, ethyl esterHCID 3703088—
SolventHexamethylphosphoramideHCID 12679—
ProductHCID 54272250HCID 54272250—

Reaction Steps

To sodium hydride (2.84 g, 57% in oil, washed with pentane), 110 ml dry THF and 20 ml HMPT, cooled to 0° and under nitrogen, is added 12.7 g ethyl 4-phenyl-3-butenoate slowly with stirring. Then 6.5 ml of isopropyliodide is added and the reaction mixture is stirred for about 60 hrs. The reaction is worked up by extracting into water/ether mixture. The aqueous phase is extracted with ether. The organic phases are combined, washed with brine, dried over calcium sulfate and rotoevaporated to give ethyl 2-isopropyl-4-phenyl-3-butenoate, which is hydrolyzed (potassium hydroxide, water-methanol) to the acid, 2-isopropyl-4-phenyl-3-butenoic acid. The acid is reacted with m-phenoxybenzyl alcohol following the procedure of Example 4 to yield m-phenoxybenzyl ester of 2-isopropyl-4-phenyl-3-butenoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04267359
Source datasetuspto-grants-1981_05
ORD IDord-073c790114004f7b93c57b06d901d478
Source noteuspto-grants-1981_05